A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516187



Internal ID20889548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4899785..4901544hg38UCSC Ensembl
chr19:4899797..4901556hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381760
hg191760
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198226
Samples
Known GenesARRDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516187
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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